Package 63323-658-20

Brand: chlorothiazide

Generic: chlorothiazide sodium
NDC Package

Package Facts

Identity

Package NDC 63323-658-20
Digits Only 6332365820
Product NDC 63323-658
Product ID 63323-658_93a228ba-a76b-43ad-9fed-2ea03a10515d
Description

1 VIAL in 1 BOX (63323-658-20) / 18 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2009-10-21
Brand chlorothiazide
Generic chlorothiazide sodium
Sample Package No

Linked Drug Pages (1)

Chlorothiazide ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "93a228ba-a76b-43ad-9fed-2ea03a10515d", "openfda": {"upc": ["0363323658205"], "unii": ["SN86FG7N2K"], "rxcui": ["484152"], "spl_set_id": ["de512e9b-444c-4ae4-8c6b-accd87a02021"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BOX (63323-658-20)  / 18 mL in 1 VIAL", "package_ndc": "63323-658-20", "marketing_start_date": "20091021"}], "brand_name": "Chlorothiazide", "product_id": "63323-658_93a228ba-a76b-43ad-9fed-2ea03a10515d", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "63323-658", "generic_name": "CHLOROTHIAZIDE SODIUM", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Chlorothiazide", "active_ingredients": [{"name": "CHLOROTHIAZIDE SODIUM", "strength": "500 mg/18mL"}], "application_number": "ANDA090896", "marketing_category": "ANDA", "marketing_start_date": "20091021", "listing_expiration_date": "20261231"}